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Old 03-24-2008, 07:23 AM #1
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That sounds like a great plan. Fingers crossed and please keep us posted. Jules
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Old 03-24-2008, 09:51 AM #2
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Thanks for posting this info, Victorya. My DD is on Topamax and the first month, she noted cog fog. But, she had her dose lowered and seems better now.

I empathize w/any one who suffers from migraines. Keep us posted on how the new meds are doing. Hope you see improvement...
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Old 03-25-2008, 12:33 PM #3
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I would be curious if you ever go on Namenda, how you feel. My doc put me on it once for pain management and my spasticity improved and I felt more fluid in movement.
Had to go off it when insurance decided it was not intended for MS. Boo
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Old 03-25-2008, 01:52 PM #4
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Good Luck and tell us how these work for you!
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